Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
The habenular volume and PDE7A allelic polymorphism in major depressive disorder: preliminary findings. / Aftanas, Lyubomir I.; Filimonova, Elena A.; Anisimenko, Maksim S. и др.
в: World Journal of Biological Psychiatry, Том 24, № 3, 03.2023, стр. 223-232.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - The habenular volume and PDE7A allelic polymorphism in major depressive disorder: preliminary findings
AU - Aftanas, Lyubomir I.
AU - Filimonova, Elena A.
AU - Anisimenko, Maksim S.
AU - Berdyugina, Darya A.
AU - Rezakova, Maria V.
AU - Simutkin, German G.
AU - Bokhan, Nikolay A.
AU - Ivanova, Svetlana A.
AU - Danilenko, Konstantin V.
AU - Lipina, Tatiana V.
N1 - Publisher Copyright: © 2022 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2023/3
Y1 - 2023/3
N2 - Objectives: The habenula is a brain structure implicated in depression, yet with unknown molecular mechanisms. Several phosphodiesterases (PDEs) have been associated with a risk of depression. Although the role of PDE7A in the brain is unknown, it has enriched expression in the medial habenula, suggesting that it may play a role in depression. Methods: We analysed: (1) habenula volume assessed by 3-T magnetic resonance imaging (MRI) in 84 patients with major depressive disorder (MDD) and 41 healthy controls; (2) frequencies of 10 single nucleotide polymorphisms (SNPs) in PDE7A gene in 235 patients and 41 controls; and (3) both indices in 80 patients and 27 controls. The analyses considered gender, age, body mass index and season of the MRI examination. Results: The analysis did not reveal habenula volumetric changes in MDD patients regardless of PDE7A SNPs. However, in the combined group, the carriers of one or more mutations among 10 SNPs in the PDE7A gene had a lower volume of the left habenula (driven mainly by rs972362 and rs138599850 mutations) and consequently had the reduced habenular laterality index in comparison with individuals without PDE7A mutations. Conclusions: Our findings suggest the implication of the PDE7A gene into mechanisms determining the habenula structure.
AB - Objectives: The habenula is a brain structure implicated in depression, yet with unknown molecular mechanisms. Several phosphodiesterases (PDEs) have been associated with a risk of depression. Although the role of PDE7A in the brain is unknown, it has enriched expression in the medial habenula, suggesting that it may play a role in depression. Methods: We analysed: (1) habenula volume assessed by 3-T magnetic resonance imaging (MRI) in 84 patients with major depressive disorder (MDD) and 41 healthy controls; (2) frequencies of 10 single nucleotide polymorphisms (SNPs) in PDE7A gene in 235 patients and 41 controls; and (3) both indices in 80 patients and 27 controls. The analyses considered gender, age, body mass index and season of the MRI examination. Results: The analysis did not reveal habenula volumetric changes in MDD patients regardless of PDE7A SNPs. However, in the combined group, the carriers of one or more mutations among 10 SNPs in the PDE7A gene had a lower volume of the left habenula (driven mainly by rs972362 and rs138599850 mutations) and consequently had the reduced habenular laterality index in comparison with individuals without PDE7A mutations. Conclusions: Our findings suggest the implication of the PDE7A gene into mechanisms determining the habenula structure.
KW - habenular volume
KW - healthy subjects
KW - magnetic resonance imaging (MRI)
KW - Major depressive disorder
KW - PDE7A allelic polymorphism
KW - Humans
KW - Habenula
KW - Magnetic Resonance Imaging/methods
KW - Polymorphism, Single Nucleotide
KW - Depressive Disorder, Major/genetics
UR - http://www.scopus.com/inward/record.url?scp=85133667182&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/68699793-962a-3a1f-9574-8d1f4532e85c/
U2 - 10.1080/15622975.2022.2086297
DO - 10.1080/15622975.2022.2086297
M3 - Article
C2 - 35673941
AN - SCOPUS:85133667182
VL - 24
SP - 223
EP - 232
JO - World Journal of Biological Psychiatry
JF - World Journal of Biological Psychiatry
SN - 1562-2975
IS - 3
ER -
ID: 36778378